US7745508B2 - Compositions and methods for coating food cans - Google Patents

Compositions and methods for coating food cans Download PDF

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Publication number
US7745508B2
US7745508B2 US10/231,652 US23165202A US7745508B2 US 7745508 B2 US7745508 B2 US 7745508B2 US 23165202 A US23165202 A US 23165202A US 7745508 B2 US7745508 B2 US 7745508B2
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composition
polyester
acid
acrylic copolymer
acrylic
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US10/231,652
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US20040044117A1 (en
Inventor
Laura Kiefer-Liptak
John M. Dudik
Ronald R. Ambrose
Kevin C. Olson
Padmanabhan Sundararaman
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PPG Industries Ohio Inc
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PPG Industries Ohio Inc
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Priority to US10/231,652 priority Critical patent/US7745508B2/en
Assigned to PPG INDUSTRIES OHIO, INC. reassignment PPG INDUSTRIES OHIO, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: KIEFER-LIPTAK, LAURA, SUNDARARAMAN, PADMANABHAN, AMBROSE, RONALD R., DUDIK, JOHN M., OLSON, KEVIN C.
Priority to AT03791622T priority patent/ATE373057T1/de
Priority to SI200331025T priority patent/SI1534793T1/sl
Priority to DK03791622T priority patent/DK1534793T3/da
Priority to DE60316308T priority patent/DE60316308T2/de
Priority to CA002496410A priority patent/CA2496410C/en
Priority to MXPA05002182A priority patent/MXPA05002182A/es
Priority to PCT/US2003/024014 priority patent/WO2004020541A1/en
Priority to CNB038203146A priority patent/CN100381521C/zh
Priority to PT03791622T priority patent/PT1534793E/pt
Priority to EP03791622A priority patent/EP1534793B1/en
Priority to ES03791622T priority patent/ES2293079T3/es
Priority to AU2003257970A priority patent/AU2003257970B2/en
Priority to KR1020057003283A priority patent/KR100821412B1/ko
Priority to US10/737,085 priority patent/US20040132895A1/en
Publication of US20040044117A1 publication Critical patent/US20040044117A1/en
Priority to HK06102106A priority patent/HK1081981A1/xx
Priority to US11/862,423 priority patent/US7803415B2/en
Priority to CY20071101424T priority patent/CY1107071T1/el
Priority to US12/781,083 priority patent/US20100222493A1/en
Publication of US7745508B2 publication Critical patent/US7745508B2/en
Application granted granted Critical
Priority to US13/370,440 priority patent/US20120138502A1/en
Priority to US13/832,034 priority patent/US9221977B2/en
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    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
    • C09D167/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
    • C09D167/03—Polyesters derived from dicarboxylic acids and dihydroxy compounds the dicarboxylic acids and dihydroxy compounds having the carboxyl - and the hydroxy groups directly linked to aromatic rings
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
    • C09D167/06—Unsaturated polyesters having carbon-to-carbon unsaturation
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
    • C08L67/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
    • C08L67/06—Unsaturated polyesters
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D151/00—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers
    • C09D151/08—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers grafted on to macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
    • C09D167/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
    • C09D167/04—Polyesters derived from hydroxycarboxylic acids, e.g. lactones
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
    • C08K5/0025—Crosslinking or vulcanising agents; including accelerators
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/16—Nitrogen-containing compounds
    • C08K5/34—Heterocyclic compounds having nitrogen in the ring
    • C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
    • C08K5/3477—Six-membered rings
    • C08K5/3492—Triazines
    • C08K5/34922—Melamine; Derivatives thereof
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
    • C08L51/08—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to macromolecular compounds obtained otherwise than by reactions only involving unsaturated carbon-to-carbon bonds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
    • C08L61/04—Condensation polymers of aldehydes or ketones with phenols only
    • C08L61/06—Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols
    • C08L61/12—Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols with polyhydric phenols
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L87/00—Compositions of unspecified macromolecular compounds, obtained otherwise than by polymerisation reactions only involving unsaturated carbon-to-carbon bonds
    • C08L87/005—Block or graft polymers not provided for in groups C08L1/00 - C08L85/04

Definitions

  • the present invention relates to compositions and methods for coating metal. More specifically, the present invention relates to compositions and methods for coating food cans, wherein the coating compositions comprise polyester and acrylic polymers.
  • epoxy-based coatings and polyvinyl chloride-based coatings have been used in the past to coat the interior of metal cans to prevent corrosion.
  • the recycling of materials containing polyvinyl chloride or related halide-containing vinyl polymers can generate toxic by-products, however; moreover, these polymers are typically formulated with epoxy-functional plasticizers.
  • epoxy-based coatings are prepared from monomers such as bisphenol A and bisphenol A diglycidylether (“BADGE”), which is being reported as having negative health effects. While attempts have been made to scavenge the residual unreacted epoxy with, for example, acid functional polymers, this does not adequately address the problem; some free BADGE or its by-products will still remain. Government authorities, particularly in Europe, are becoming even more restrictive on the amount of free BADGE or its by-products that are acceptable. Thus, there is a need for food and beverage can liners that are virtually free from BADGE, epoxy and vinyl products.
  • the present invention is directed to compositions and methods for coating the inside of food cans.
  • food cans is used herein to refer to cans, containers or any type of metal receptacle used to hold any type of food or beverage.
  • the methods generally involve coating the cans with a composition comprising a polyester and an acrylic polyol.
  • polyester coatings are good for flexibility, but are subject to hydrolysis in acid environments.
  • acrylics are good for providing resistance, but are inflexible.
  • the present invention is directed to compositions for coating food cans comprising an acrylic copolymer; a polyester; and a crosslinker.
  • the polyester and acrylic copolymer should be made compatible to form the present compositions. This can be accomplished by any of various methods known in the art or described herein, including but not limited to employing blending techniques known in the art, preparing interpenetrating networks, or forming a graft copolymer.
  • the compositions are “epoxy-free”. “Epoxy-free” means that both the polyester and acrylic portion of the composition are free from oxirane rings or residues of oxirane rings; bisphenol A; BADGE or adducts of BADGE.
  • the coating composition is also free of polyvinylchloride or related halide-containing vinyl polymers.
  • the polyester component used in the present methods can be prepared by conventional means such as polyesterification of a polycarboxylic acid or anhydride with a polyol using techniques known to those skilled in the art.
  • the polycarboxylic acids and polyols are aliphatic or aromatic dibasic acids and diols, although the invention is not so limited. Transesterification of polycarboxylic acid esters using conventional techniques is also possible.
  • the weight average molecular weight (“Mw”) of the polyester will range from 4,000 to 20,000, such as 5,000 to 13,000, or 7,000 to 11,000.
  • the polyester will typically have a hydroxy value of from 0 to 200 mg KOH/g resin, such as from 30 to 70, or about 40, and an acid value of less than about 10, such as less than 5.
  • any polyols known to be suitable for making the polyesters can be used to form the polyester component of the present compositions.
  • alkylene glycols such as ethylene glycol, propylene glycol, diethylene glycol, dipropylene glycol, triethylene glycol, tripropylene glycol, hexylene glycol, polyethylene glycol, polypropylene glycol and neopentyl glycol; hydrogenated Bisphenol A; cyclohexanediol; 1,3-propane diol; glycol; 1,4-butane diol; 1,3-butane diol; butyl ethyl propane diol; trimethyl pentane diol; cyclohexanedimethanol; caprolactonediol, for example, the reaction product of epsilon-caprolactone and ethylene glycol; hydroxy-alkylated bisphenols; polyether glycols, for example, poly(oxytetramethylene
  • Polyols of higher functionality may also be used in limited quantity, provided they have no adverse effects on flexibility. Examples include trimethylolpropane, trimethylolethane, pentaerythritol, tris-hydroxyethylisocyanurate and the like.
  • any mono or polyacid known for use in the preparation of polyesters can be used to prepare the polyester polymer component of the present invention, and can include, for example, monomeric carboxylic acids or anhydrides having 2 to 18 carbon atoms per molecule.
  • Examples include phthalic acid, isophthalic acid, 5-tert-butyl isophthalic acid, endomethylene tetrahydrophthalic acid, tetrachlorophthalic anhydride, chlorendic acid, naphthalene dicarboxylic acid, terephthalic acid, tetrahydrophthalic acid, hexahydrophthalic acid, methylhexahydrophthalic acid, 1,3-cyclohexane dicarboxylic acid, 1,4-cyclohexane dicarboxylic acid, adipic acid, azelaic acid, sebacic acid, maleic acid, fumaric acid, itaconic acid, succinic acid, glutaric acid, decanoic diacid, do
  • the polyester may include minor amounts of monobasic acids such as benzoic acid, stearic acid, acetic acid and oleic acid. Also, there may be employed higher carboxylic acids, such as trimellitic acid and tricarballylic acid. Where acids are referred to above, it is understood that anhydrides thereof that exist may be used in place of the acid. Also, lower alkyl esters of diacids such as dimethyl glutarate and dimethyl terephthalate can be used.
  • the present polyester components are unsaturated. While any unsaturated polyester can be used according to the present invention, a particularly suitable polyester is formed from butanediol, ethylene glycol, cyclohexane dicarboxylic acid, isophthalic acid and maleic anhydride. This embodiment is particularly suitable when a graft copolymer is made between the polyester and acrylic copolymer; maleic anhydride, which is not typically incorporated into the polyesters, promotes grafting with the acrylic copolymer. Maleic acid, fumaric acid and/or itaconic acid and/or the anhydrides of these acids can also be used instead of or in addition to maleic anhydride to produce polyesters that also have components particularly suitable for graft promotion. In certain instances, the polyester of this embodiment is also particularly desirable, as all of the components of the polyester are approved by the United States Food and Drug Administration (“FDA”) for direct food contact; these components are also listed on the European Inventory of Existing Commercial Substances (“EINECS”).
  • FDA United States Food
  • the polyester is made with excess polyol as compared with acid so as to produce a polyester that has hydroxy functionality.
  • the polyester can also be prepared so as to either lack or have acid functionality.
  • acrylic monomers can be combined to prepare the acrylic copolymer used in the present invention.
  • examples include methyl(meth)acrylate, ethyl(meth)acrylate, butyl(meth)acrylate, 2-ethylhexyl(meth)acrylate, (meth)acrylic acid, vinyl aromatic compounds such as styrene and vinyl toluene, nitriles such as (meth)acrylonitrile, and vinyl esters such as vinyl acetate. Any other acrylic monomers known to those skilled in the art could also be used.
  • the term “(meth)acrylate” and like terms are used conventionally and herein to refer to both methacrylate and acrylate.
  • a particularly suitable acrylic copolymer is formed with styrene, butyl acrylate, ethylhexyl acrylate and methacrylic acid, either alone or in further combination with hydroxyethyl methacrylate and methylmethacrylate.
  • this acrylic copolymer comprises components approved by the FDA for use with food cans, and listed on EINECS.
  • the Mw of the acrylic copolymer will range from about 10,000 to 250,000, such as 20,000 to 150,000, or 25,000 to 100,000.
  • the acrylic copolymer and polyester used in the present composition can be treated in any manner so as to render the two compatible.
  • compatible is meant that the polyester and the acrylic copolymer may be combined together in a coating without phase separation, thus forming a homogeneous product.
  • Compatibilized copolymers can simply be blended together. In this blended embodiment, the acrylate copolymer used according to the present invention does not have pendant glycidyl groups when the polyester is acid terminated, and the acrylate copolymer does not have pendant hydroxy groups when the polyester is hydroxy terminated.
  • Compatibilization can be achieved, for example, by using an acrylic copolymer having an Mw similar to the Mw of the polyester (i.e. within about 1,000).
  • the acrylic copolymer can have N-(N-butoxymethyl)acrylamide (“NBMA”) functionality.
  • NBMA N-(N-butoxymethyl)acrylamide
  • Other compatibilizing functional groups include acid functional groups, hydroxy groups, amide groups and the like.
  • Appropriate solvents referred to in the art as “coupling solvents” can also aid in compatibilization.
  • An example is ethylene glycol monobutyl ether, commercially available as Butyl Cellosolve from Dow Chemical.
  • the acrylate copolymer and polyester can also be compatibilized, for example, by forming interpenetrating polymer networks.
  • the preparation of such networks is described, for example, in U.S. Pat. No. 6,228,919, incorporated by reference herein.
  • a graft copolymer can be formed using techniques standard in the art.
  • the polyester is prepared according to conventional methods using the materials described above.
  • the acrylic monomers are then added to the polyester.
  • the acrylic can then be polymerized using a standard free radical initiator. In this manner, the acrylate copolymer is grafted to the already-made polyester.
  • the polyester can be grafted to an already-made acrylic copolymer.
  • a maleic anhydride group can be polymerized in the acrylic copolymer and, subsequently, hydroxyl groups from the polyester can be allowed to react with the acrylic to create a graft copolymer; the result will be an acrylic copolymer having polyester moieties grafted thereto.
  • a particularly suitable example uses maleic anhydride in the formation of a polyester and styrene as one of the acrylic monomers.
  • the styrene will react with the maleic anhydride; the acrylic copolymer will grow off of the styrene through the formation of free radicals.
  • the result will be a polyester having acrylic copolymers grafted thereto. It will be appreciated that not all of the acrylic and polyester will graft; thus, there will be some “neat” polyester and some “neat” acrylate copolymer in the solution. Enough of the acrylate copolymer and polyester will graft, however, to compatibilize the two normally incompatible polymers.
  • maleic anhydride and styrene are offered as examples of two components that will promote grafting between the normally incompatible polymers, but that the invention is not so limited.
  • Other compounds such as fumaric acid/anhydride or itaconic acid/anhydride may be incorporated into a polyester for grafting with a styrene containing acrylic.
  • Other moieties that will promote grafting between the polyester and acrylic can also be used. Any group of compounds can be used for this purpose. All of these compounds are referred to herein as “graft promoting components”.
  • the amount of graft promoting component used in each of the polyester and/or acrylate portions can affect the final product. If too much of these components are used, the product can gel or be otherwise unusable.
  • the graft-promoting components should therefore be used in an amount effective to promote grafting but not to cause gelling. Enough grafting should be effected to allow the polyester and acrylate polymers to be compatible.
  • Enough grafting should be effected to allow the polyester and acrylate polymers to be compatible.
  • usually 2 to 6 weight percent maleic with 8 to 30 weight percent styrene can be used, with weight percent being based on the weight of the polyester and the weight of the acrylic, respectively.
  • the Mw of the graft copolymer will typically be from about 3000 to 250,000, such as from about 5000 to 125,000, or from about 30,000 to 50,000.
  • the weight ratio of polyester to acrylic in the present compositions can vary widely.
  • the polyester to acrylic ratio can range from 95:5 to 20:80. It has been determined that varying the amount of polyester in the composition will affect the amount of flexibility.
  • a particularly suitable ratio of polyester to acrylic for use in coating food cans is 70:30, which gives a relatively flexible product that still has suitable acid resistance.
  • a suitable crosslinker can be determined based upon the needs and desires of the user, and can include, for example, melamine crosslinkers, and phenolic crosslinkers. Melamine crosslinkers are widely commercially available, such as from Cytec Industries, Inc. as CYMEL 303, 1130, 325, 327 and 370. Phenolic crosslinkers include, for example, novolacs, resoles, and bisphenol A. Preferred for use on food cans are phenolic resoles that are not derived from bisphenol A.
  • compositions of the present invention also comprise a solvent.
  • suitable solvents include esters, glycol ethers, glycols, ketones, aromatic and aliphatic hydrocarbons, alcohols and the like. Particularly suitable are zylenes, propyleneglycol monomethyl acetates, and dibasic esters such as dimethyl esters of adipic, glutaric and succinic acids.
  • the compositions are prepared so as to be between about 30 and 50 weight percent solids.
  • compositions of the present invention can also contain any other conventional additives such as pigments, colorants, waxes, lubricants, defoamers, wetting agents, plasticizers, fortifiers and catalysts.
  • Any mineral or sulfonic acid catalyst can be used. Particularly preferred for food can applications are phosphoric acid and dodecyl benzene sulfonic acid.
  • the present invention is further directed to a method for coating food cans comprising applying any of the compositions described above to the food can. More specifically, these compositions comprise a polymer, an acrylic copolymer, a crosslinker, one or more solvents and optionally one or more conventional additives.
  • the polyester and acrylic copolymer can be made compatible by any means described above such as using blending techniques known in the art, interpenetrating networks, or the novel graft copolymerizations described herein.
  • the coating composition can be applied to the food can by any means known in the art such as roll coating, spraying, and electrocoating. It will be appreciated that for two-piece food cans, the coating will typically be sprayed after the can is made. For three-piece food cans, on the other hand, a coil or sheet will typically be roll coated with one or more of the present compositions first and then the can will be formed.
  • Cure is effected by methods standard in the art. For coil coating, this is typically a short dwell time (i.e. 9 seconds to 2 minutes) at high heat (i.e. 485° F. peak metal temperature); for coated metal sheets cure is typically longer (i.e. 10 minutes) but at lower temperatures (i.e. 400° F. peak metal temperature).
  • Any material used for the formation of food cans can be treated according to the present methods.
  • Particularly suitable substrates include tin-plated steel, tin-free steel, and black-plated steel.
  • the coatings of the present invention can be applied directly to the steel, without any pretreatment or adhesive aid being added to the metal first. In addition, no coatings need to be applied over top of the coatings used in the present methods.
  • compositions of the present invention perform as desired both in the areas of flexibility and acid resistance. Significantly, these results can be achieved with an epoxy-free composition.
  • present invention provides particularly desirable compositions and methods for coating food cans, which avoid performance and health issues raised by other coatings and methods reported in the art.
  • the present invention provides methods for compatibilizing a polyester and an acrylic. These methods are discussed above and include, for example, the use of an acrylamide in the formation of the acrylic copolymer, and the graft copolymerization of an acrylic onto a polyester or a polyester onto an acrylic.
  • polymer refers to oligomers and both homopolymers and copolymers, and the prefix “poly” refers to two or more.
  • Polyester Polymer “A” was made as follows:
  • Polyester Polymer “B” was made as follows:
  • Charge #1 was added to a 5 liter, 4 necked flask equipped with a motor driven stainless steel stir blade, a packed column connected to a water-cooled condenser and a heating mantle with a thermometer connected through a temperature feedback control device.
  • the reaction mixture was heated to 125° C.
  • Charge #2 was added to the mixture and then heated to 155° C. Distillation of water began and continued for 3.5 hours.
  • the temperature was increased to 175° C. for 90 minutes and then to 195° C. for four hours.
  • the reaction temperature was increased to 200° C. for 3.5 hours where the distillation of water began to significantly slow.
  • the reaction mixture was cooled to 180° C., the packed column replaced with a Dean-Stark and a nitrogen sparge was started.
  • Charge #3 was added and the reaction was heated to 195° C. for seven hours at which time the acid value was less than 2.0.
  • the resin was cooled to 80° C. and then thinned with Charge #4.
  • Acrylic Polyester Copolymer “A” was made as follows:
  • Charge #1 was added to a 3 liter, 4 necked flask equipped with a motor driven stainless steel stir blade, water-cooled condenser and a heating mantle 15 with a thermometer connected through a temperature feedback control device.
  • the contents of the flask were heated to reflux (128° C.).
  • Addition of Charge #2 (over 190 minutes) began followed by the addition of Charge #3 (over 180 minutes) five minutes later.
  • the reflux temperature gradually rose to 138° C.
  • Charge #4 was added over 10 minutes and the mixture was held at 138° C. for an additional hour.
  • the resin was thinned with Charge #5.
  • Acrylic Polyester Copolymer “B” was made as follows:
  • Charge #1 was added to a 2 liter, 4 necked flask equipped with a motor driven stainless steel stir blade, water-cooled condenser and a heating mantle with a thermometer connected through a temperature feedback control device. The contents of the flask were heated to reflux (150° C.). Addition of Charges #2 and #3 were started simultaneously and continued over three hours. After the additions were complete, the reaction was held at 150° C. for 30 minutes. Charges #4, 5, 6 and 7 were then added to the mixture in 30-minute increments. After Charge #7 was added, the mixture was held for 30 additional minutes, was cooled to 130° C. and Charge #8 was added.
  • Acrylic Polyester Copolymer “C” was made as follows:
  • Charge #1 was added to a 2 liter, 4 necked flask equipped with motor driven stainless steel stir blade, water cooled condenser and a heating mantle with a thermometer connected through a temperature feedback control device. The contents of the flask were heated to 128° C. Addition of Charge #2 (over 190 minutes) followed by Charge #3 (over 180 minutes) five minutes later. After the additions were complete, the reaction was held at 150° C. for 30 minutes. During the additions, the temperature was gradually increased reflux at 138° C. After the additions were complete, the reaction was held at 138° C. for 90 minutes. Charge #4 was then added over 10 minutes followed by a one hour hold at 138° C. The resin was then thinned with Charge #5 and then cooled.
  • Coatings were prepared by drawing Samples 1-3 and a commercially available epoxy liner for food cans (Eurogold XF 12040, from PPG Industries, Inc.) over tin plated steel (E.T.P.) sheets with a #12 wire-wound rod. The coatings were baked for 10.5 minutes at 400° F. The drying coating weights were 4.0 mgs/sq.in.
  • the coated sheets were evaluated for flexibility by bending and stamping wedges (2.0 inch by 4.5 inches), stamping 300 food can ends, and by drawing cups to 18 mm and 26 mm depths with one and two stages of drawing, respectively.
  • the percent of coating that remained crack-free along the bend radius (for wedge bends) and along the drawn lengths (for cups) was determined.
  • the measured current (in mA) was determined using a WACO enamel rater (obtained from Wilkens-Anderson Company) in 4 sec mode using an electrolyte solution of 7.0 grams of potassium ferrocyanurate, 5.4 grams of sodium chloride, 0.5 grams of sodium sulfosuccinate, and 1000 grams of water.
  • the resistance properties of the coated stamped ends and drawn cups were evaluated by processing (retorting) them in three food simulants and measuring their ability to resist current (stamped ends) and cracking (drawn cups) after one hour in a sterilizer under 266° F./30 psi conditions.
  • the three simulants were tap water, a 1% by weight solution of sodium chloride in tap water, and a 1% by weight solution of lactic acid in tap water. All of the results are presented in Table 7.
  • Sample 1 had better results than did a current, epoxy-containing food can liner.
  • Sample 2 also had very good results, especially acid resistance.
  • Both Samples 1 and 2 had polyester to acrylic ratios of about 70:30.
  • Sample 3, which had a polyester to acrylic ratio of 20:80 demonstrates that some flexibility can be lost with lower levels of polyester.

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MXPA05002182A MXPA05002182A (es) 2002-08-30 2003-07-31 Composiciones y metodos para recubrir latas para alimentos.
PCT/US2003/024014 WO2004020541A1 (en) 2002-08-30 2003-07-31 Compositions and methods for coating food cans
CNB038203146A CN100381521C (zh) 2002-08-30 2003-07-31 涂布食品罐的组合物和方法
PT03791622T PT1534793E (pt) 2002-08-30 2003-07-31 Composições e métodos para o revestimento de latas de conserva
EP03791622A EP1534793B1 (en) 2002-08-30 2003-07-31 Compositions and methods for coating food cans
ES03791622T ES2293079T3 (es) 2002-08-30 2003-07-31 Composiciones y procedimientos para revestir latas para alimentos.
AT03791622T ATE373057T1 (de) 2002-08-30 2003-07-31 Zusammensetzungen und verfahren zur beschichtung von konservendosen
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US10/737,085 US20040132895A1 (en) 2002-08-30 2003-12-16 Compositions and methods for coating food cans
HK06102106A HK1081981A1 (en) 2002-08-30 2006-02-17 Compositions and methods for coating food cans
US11/862,423 US7803415B2 (en) 2002-08-30 2007-09-27 Methods for coating food cans
CY20071101424T CY1107071T1 (el) 2002-08-30 2007-11-07 Συνθεσεις και μεθοδοι για την επικαλυψη κονσερβων τροφων
US12/781,083 US20100222493A1 (en) 2002-08-30 2010-05-17 Compositions and methods for coating food cans
US13/370,440 US20120138502A1 (en) 2002-08-30 2012-02-10 Compositions and methods for coating food cans
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US8465846B2 (en) 2003-04-02 2013-06-18 Valspar Sourcing, Inc. Aqueous dispersions and coatings
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EP2806001A1 (en) 2013-05-21 2014-11-26 PPG Industries Ohio Inc. Coating composition
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US9133292B2 (en) 2009-03-05 2015-09-15 Akzo Nobel Coatings International B.V. Hydroxyl functional oil polyol acrylic graft copolymers
US9260625B2 (en) 2011-12-21 2016-02-16 Akzo Nobel Coatings International B.V. Water-based coating compositions
US9273226B2 (en) 2011-12-21 2016-03-01 Akzo Nobel Coatings International B.V. Solvent-based coating compositions
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US9415900B2 (en) 2004-10-20 2016-08-16 Valspar Sourcing, Inc. Coating compositions for aluminum beverage cans and methods of coating same
US8617663B2 (en) 2004-10-20 2013-12-31 Valspar Sourcing, Inc. Coating compositions for cans and methods of coating
US8835012B2 (en) 2004-10-20 2014-09-16 Valspar Sourcing, Inc. Coating compositions for aluminum beverage cans and methods of coating same
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US9862854B2 (en) 2004-10-20 2018-01-09 Valspar Sourcing, Inc. Coating compositions for aluminum beverage cans and methods of coating same
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US9260625B2 (en) 2011-12-21 2016-02-16 Akzo Nobel Coatings International B.V. Water-based coating compositions
US9273226B2 (en) 2011-12-21 2016-03-01 Akzo Nobel Coatings International B.V. Solvent-based coating compositions
EP2806001A1 (en) 2013-05-21 2014-11-26 PPG Industries Ohio Inc. Coating composition
EP2865721A1 (en) 2013-10-25 2015-04-29 PPG Industries Ohio Inc. A coating composition
US11708444B2 (en) 2016-12-12 2023-07-25 Ppg Industries Ohio, Inc. Acrylic polyester resin and an aqueous coating composition containing the same
US11981764B2 (en) 2016-12-12 2024-05-14 Ppg Industries Ohio, Inc. Acrylic polyester resin and an aqueous coating composition containing the same
US12018110B2 (en) 2018-06-20 2024-06-25 Ppg Industries Ohio, Inc. Acrylic polyester resin and an aqueous coating composition containing the same
US12104073B2 (en) 2018-07-25 2024-10-01 Ppg Industries Ohio, Inc. Product coated with an aqueous or powder coating composition comprising an acrylic polyester resin

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US20100222493A1 (en) 2010-09-02
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EP1534793B1 (en) 2007-09-12

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